Canonical Allele Identifier: CA1846870560

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429792G= , CM000671.2:g.37429792G=	GRCh38
NC_000009.11:g.37429789G= , CM000671.1:g.37429789G=	GRCh37
NC_000009.10:g.37419789G=	NCBI36
NG_008135.1:g.12083G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.554G= MANE Select	ENSP00000313432.6:p.Arg185=
ENST00000318158.10:c.554G=	ENSP00000313432.6:p.Arg185=
ENST00000377824.8:n.591G=
ENST00000460882.5:n.581G=
ENST00000480596.5:n.1255G=
ENST00000482603.1:n.7G=
ENST00000491488.5:n.259G=
ENST00000494290.1:c.125G=	ENSP00000432021.1:p.Arg42=
ENST00000497693.1:n.2087G=
ENST00000607784.1:c.554G=	ENSP00000475569.1:p.Arg185=
NM_012203.1:c.554G=	NP_036335.1:p.Arg185=
XM_005251631.1:c.233G=	XP_005251688.1:p.Arg78=
XM_011518073.1:c.152G=	XP_011516375.1:p.Arg51=
XR_929374.1:n.999G=
XM_017015320.2:c.554G=	XP_016870809.1:p.Arg185=
XM_017015321.2:c.554G=	XP_016870810.1:p.Arg185=
XM_017015323.2:c.152G=	XP_016870812.1:p.Arg51=
XM_024447716.1:c.827G=	XP_024303484.1:p.Arg276=
XM_024447717.1:c.827G=	XP_024303485.1:p.Arg276=
XR_002956828.1:n.842G=
XR_002956829.1:n.842G=
XR_002956830.1:n.613G=
XR_002956831.1:n.288G=
XR_002956832.1:n.973G=
NM_012203.2:c.554G= MANE Select	NP_036335.1:p.Arg185=